Department of Pathology and Laboratory Medicine, Memorial Sloan Kettering Cancer Center, New York, New York.
Scisco Genetics Inc., Seattle, Washington.
J Mol Diagn. 2024 Nov;26(11):995-1006. doi: 10.1016/j.jmoldx.2024.07.003. Epub 2024 Aug 22.
Chimerism analysis by next-generation sequencing (NGS) is an emerging method for engraftment monitoring after allogeneic hematopoietic cell transplantation. A high-sensitivity method is required for the detection of microchimerism (<1% chimerism), which may have clinical utility in early relapse detection, allograft monitoring in organ transplantation, and other allogeneic cellular therapies (such as microtransplantations). As more clinical laboratories adopt this method, a thorough assessment of performance is needed. This study evaluated one such NGS-based assay that uses both single-nucleotide polymorphisms and insertions/deletions as genetic markers. An assessment of accuracy, linearity, sensitivity, and reproducibility was performed. Analytical sensitivity was 0.2% donor for single donor and 0.5% donors for double donors. The assay showed a high degree of reproducibility over a full range of chimerism. Comparison to short-tandem-repeat (STR) PCR showed high concordance; yet <5% chimerism was consistently detected by NGS, but not by STR-PCR. Comparison to real-time quantitative PCR showed high concordance, but with lower correlation in the midrange (40% to 60% chimerism). Overall, the assay showed consistent performance with high sensitivity and accuracy compared with STR-PCR and real-time quantitative PCR across a full range of chimerism in the setting of single-donor and multidonor transplantations. In addition, criteria for quality metrics were established for sequencing performance and data analysis and considerations made for clinical laboratory validation of NGS-based chimerism assay and analysis software.
基于下一代测序(NGS)的嵌合体分析是一种新兴的异基因造血细胞移植后植入监测方法。需要一种高灵敏度的方法来检测微嵌合体(<1%嵌合体),这在早期复发检测、器官移植中的同种异体移植物监测以及其他同种异体细胞治疗(如微移植)中可能具有临床应用价值。随着越来越多的临床实验室采用这种方法,需要对其性能进行全面评估。本研究评估了一种基于 NGS 的检测方法,该方法同时使用单核苷酸多态性和插入/缺失作为遗传标记。对准确性、线性、灵敏度和重现性进行了评估。分析灵敏度对于单供体为 0.2%,对于双供体为 0.5%。该检测方法在整个嵌合体范围内显示出高度的重现性。与短串联重复序列(STR)PCR 的比较显示出高度的一致性;然而,NGS 可以检测到<5%的嵌合体,但 STR-PCR 却无法检测到。与实时定量 PCR 的比较显示出高度的一致性,但在中范围(40%至 60%嵌合体)的相关性较低。总体而言,与 STR-PCR 和实时定量 PCR 相比,该检测方法在单供体和多供体移植中,在整个嵌合体范围内表现出一致的性能,具有较高的灵敏度和准确性。此外,还为测序性能和数据分析制定了质量指标标准,并考虑了对基于 NGS 的嵌合体检测和分析软件的临床实验室验证。